Elevator number 19 M, number 510 left roots/bottom - Hu-Friedy - Delynov

What is the elevator #19 M. #510 left from Hu-Friedy?

The elevator #19 M. #510 left is a precision instrument manufactured by Hu-Friedy Mfg. Co., LLC. It is a manual device specifically configured for dental extraction procedures. Its structure is adapted to meet the needs of dental surgeons when manipulating hard tissues. This particular model is oriented for left-side use to address the anatomical constraints encountered during mandibular surgeries. As a product from a recognized manufacturer like Hu-Friedy, this instrument integrates into standardized oral surgery protocols for root management.

What are the clinical indications for this instrument?

This instrument is primarily indicated for the luxation and extraction of roots or root fragments. More specifically, it is used as a lower root elevator to treat mandibular areas. Its design is optimized for practitioners seeking a left root elevator capable of accessing lower alveolar spaces. It is used in the initial phases of extraction to break ligament fibers and mobilize the root before using forceps, or to remove fractured apices. Its use is strictly reserved for healthcare professionals qualified in dental and implant surgery.

What are the technical characteristics of this elevator?

The elevator #19 M. #510 left from Hu-Friedy is characterized by a robust design adapted to the leverage forces required in oral surgery. Although specific materials are not detailed in the technical data sheet, Hu-Friedy is renowned for the quality of its metal alloys. The instrument is classified as a Class I device according to current regulations. Its morphology is specifically designed for the extraction of mandibular roots, offering a left angulation to facilitate access to the corresponding lower quadrants. It belongs to the CONSO category of reusable devices after appropriate sterilization according to standard hospital protocols.

What are the contraindications for the use of this device?

According to information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, the use of this instrument is exclusively reserved for healthcare professionals. There are no specific medical contraindications listed in the technical documentation beyond those related to classic surgical extraction procedures. However, the practitioner must systematically refer to the instructions for use before any intervention. As with any Class I instrument, a visual inspection before use is recommended to ensure the integrity of the device and avoid any risk related to premature wear or structural damage.

What are the maintenance and storage precautions?

Being a non-resorbable instrument intended for surgery, the mandibular root elevator must undergo a complete cycle of cleaning, disinfection, and sterilization between each patient. Hu-Friedy recommends strictly following the reprocessing instructions provided by the manufacturer to guarantee the longevity of the instrument and the safety of care. It is essential to check for the absence of organic residues before autoclave sterilization. Storage must be in a dry and clean environment, protected from any contamination. Compliance with these precautions ensures the maintenance of the steel's mechanical properties during luxation maneuvers.

Who is the manufacturer and what standards are respected?

The elevator is manufactured by Hu-Friedy Mfg. Co., LLC, headquartered at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is listed as Class I, which corresponds to the regulatory standards for non-invasive or temporary-use invasive manual surgical instruments. Hu-Friedy is a globally recognized manufacturer in the dental sector for its adherence to rigorous manufacturing standards. Although specific CE marking is not mentioned in the source data, compliance with Class I requirements guarantees a level of safety and performance adapted to the requirements of professional oral surgery.

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